RS772721937 MRPS23

Health Risk Chr 17:57849336
Upload your DNA to see your genotype for this variant.
Associated Conditions
Combined oxidative phosphorylation deficiency 46
Inborn genetic diseases
Combined oxidative phosphorylation deficiency 46
Combined oxidative phosphorylation deficiency 46
Inborn genetic diseases
Combined oxidative phosphorylation deficiency 46
Ask Dr. Hemsworth about this variant